| Tag | Content |
|---|
EnhancerAtlas ID | HS104-62140 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr9:131928930-131931380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFK | MA0496.2 | chr9:131930506-131930525 | AATTGCTGAGTCACCGTAT | + | 6.06 | | NFE2L1 | MA0089.2 | chr9:131930507-131930522 | ATTGCTGAGTCACCG | - | 6.97 | | Nfe2l2 | MA0150.2 | chr9:131930509-131930524 | TGCTGAGTCACCGTA | - | 6.68 | | ZNF263 | MA0528.1 | chr9:131930757-131930778 | GCCACCCCCACCCCCTCCCCC | - | 6 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_01377 | chr9:131928873-131930959 | Adrenal_Gland | | SE_26914 | chr9:131928223-131931145 | Esophagus | | SE_27869 | chr9:131928909-131930745 | Fetal_Intestine | | SE_28773 | chr9:131928727-131930857 | Fetal_Intestine_Large | | SE_30321 | chr9:131928839-131930038 | Fetal_Muscle | | SE_31776 | chr9:131928375-131931171 | Gastric | | SE_34379 | chr9:131928204-131931924 | HCT-116 | | SE_35053 | chr9:131928605-131931608 | HeLa | | SE_42081 | chr9:131928958-131929830 | LNCaP | | SE_42081 | chr9:131929901-131930683 | LNCaP | | SE_43197 | chr9:131928798-131930727 | Lung | | SE_46983 | chr9:131928949-131929438 | Ovary | | SE_46983 | chr9:131929455-131929836 | Ovary | | SE_46983 | chr9:131930089-131930539 | Ovary | | SE_47992 | chr9:131928939-131929430 | Pancreas | | SE_47992 | chr9:131929486-131929890 | Pancreas | | SE_47992 | chr9:131929957-131930610 | Pancreas | | SE_50677 | chr9:131928813-131930770 | Sigmoid_Colon | | SE_53874 | chr9:131928804-131930748 | Spleen | | SE_56721 | chr9:131928843-131931262 | u87 | | SE_57142 | chr9:131929046-131929865 | VACO_400 | | SE_57142 | chr9:131929927-131930596 | VACO_400 | | SE_57775 | chr9:131928926-131929839 | VACO_503 | | SE_57775 | chr9:131930005-131930538 | VACO_503 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr9 | 131929981 | 131930820 | | chr9 | 131930838 | 131930916 | | chr9 | 131928947 | 131929843 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129166 | chr9 | 131928464 | 131931823 |
|
Enhancer Sequence | CTCAGGAGGC TCAGGCAGTA GAATTGCTTG AACCTGGGAG GCGGAGGTTT CGGTGAGCTG 60
AGATCCTGGG CAACAAGAGC AAAACTGTGT CTCAAAAAAA AAAAAAAGAA AAAAAAAAGC 120
AGCAGAGCAT GGTTTGTCTT GAGCTCTATG TGGCTTTGGA GGCTGAGCTT GGAACTGCCA 180
GCCTGGGCTT TGGACGGGCA CCCTGGGTAG GGGTGGTCCT GGGTAGAGAT GGCCCTGGGA 240
ATCCCTCCGG TGCTTGGCCT TGTGCCTGGT GGTCCACAGT CTCACAGTCA CTCATCTGAT 300
ATTTAACAAC TTACAATGAG GAGTGCTCCA CAAGGAACCC TCACATAGCT TGGGATGCTC 360
TCCCATGTTC CGTCTTTGCT GAGGGTCCCT TGGATGGGTG TGTTTGTGGG GCATAGTCTC 420
TGGGGGAAGA GGGGCAGATC CTGGATTGGT CTGGAGCCCC AGCTGGCCCC GCACAACTAG 480
GAAAACTGGT TGGGGCGGCT GACTCAGGGT GTGTTTATAC TGGCGTACTC CCCGCCCCCT 540
CCCTCCCTCA GGCACCCTCC CCTCCCGTCC CTGACCCGGG AGAGGAAGGA AGTTCCTATA 600
ACGTTCATAG TTGCCACTAG TTCTGCGTGT TGTGCATTGG GCACGGAGCA GGAAGACCTT 660
CACAGGTTGT AACTGGTCCC AGCTTCCTTT GAGGAGACTG AGTCTCAGAA AAGTCAGGCT 720
GCTCCCTCGA TCCTACAGGG GCAAAGCTGG GATTGGAATC CAGCTCTGAC TGATGCCCCG 780
GATGGAACTC TCATCCACTG TGATTAGAAT ACAATCTGAG CACCTCCTGC TTTTCTTTCT 840
GGCCCCATCT CCTGCCTCTC CCACTTGCCC TCTCTCTCAG CCAGTTCTAT GAACATGCTA 900
AATTTATTCA TTTTCTTTTT TTTCTCTCTC TCTCCTTTCT TTTCTTCTTC TTTTTTTTTT 960
TTTTTTTTTT TTGCCGGAGT TTCGTTCTTC TTGCCCTGGC TAGAGTGCAA TGGTGTGATC 1020
TTGGCTCACT GCAACCTCCG CCTCCCGGGT TCAAGCGATT CTCCTCTGTC AGTCCCCCAA 1080
GTGGCTGGGA TTACAGGTGC ACACACCAGC ATGCCCAGCC AATTTTTGTA TTTTTAGTAG 1140
AGACAGGGTT TCGCCATGCT GGCCAGGCTG GTCTCACCCT GACTTCAGGT GATCTGCTCG 1200
CCTTGGCCTC CCAAAGTGCT GGGATTAAGG CGTGGGCCAC CGCGCCTGGC CTCATGTGTT 1260
TAGTCTTCAC CTTTTCCGTT CCTTCTGCCT GGAATGCTCC TCCACCGTTG TTTGTCCAGC 1320
TGCTATGGTA GAGACTTCTA GCGCTCATCC ATGTGTACTC GCCTTTCCTT CCCAGTTACC 1380
CAAGAAAACT GCTTTTCCCA GCCCCCTTGC AGTTAGATGA GGGCCTGGGA CTCATTCTGG 1440
CCAATGTGCT CTGAGTGTGA GTGAGGAGAA TCACTTCCAG GCTGAGGCCA TGAAGAGCCC 1500
TTGCAGGACT CCCCAGCTCT CATTCTGTGC CACGGTGGAG ATTCTGGAAG CCTTGTGTTG 1560
AGATAGACGC AGGCTGAATT GCTGAGTCAC CGTATGGAGG GCAGCAGCCT AGGAGACCTG 1620
GCAGTCTGAC TCAGACTTTG CATGGTCAAG AAACAAATCC TTTCTACCTG CTGGAGATCT 1680
TAAAAGAGAA AGAAATCCTT GTGTTAAATC TTTGAGATGC AGGGATTAAT TTGTTACTGC 1740
AGCATAGCCT GTCGTATACT AATAGAGCTG ATCTGTTCAG GTGTCAGTTG AAATATCACC 1800
TTCTCTGATC AAAATATCTA AACTGGTGCC ACCCCCACCC CCTCCCCCTC CAACCAGTCC 1860
TTTCTTTTTT TTTGAGACTT TTTTTTTTTG AGTCTCGTTC TGTCATCCAG GCTGGGGTGC 1920
AATGGTGCTG TGATCTTGGC TCACTCCAGC AGCTGCTTCC TAGGTGCAAG TGATTCTCCT 1980
GTCTCACTTT CCGAGTAGCT GGGATTACAG GCACGCGCCT CCACGCTAGG CTAATTTTTG 2040
TATGTTTGGT AGAGACGGGG TTTCACCATG TTGGCCAGGC CGGTCTTAAA CTCCTGGCCT 2100
CAACTGATCA GCTCACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACGGGC 2160
CCTTACCAAT TTTTCTAGCA CTGTGTTTAT TTTCCTGAAA CACTTATCTA CTTGTTTGTT 2220
GCCTTGTGTA TTGTCTGCAC ACCTCCCCCC ACCACTAGAA TGTAAGCTCT ATGAGGGGAG 2280
GGCCCTTCGT TTGTCTTGTT CATGGCTGCA TCCTTGGTGC CTAGCACAGT GCCTGGCATA 2340
TATAGGTACT CAATAAATAT TTGAATGGGT GAATGTGTGT ATATTTATTT TTTGAGACAA 2400
GGTCTCACTG TCACTAAGGC TGGAGCGCAG TGGTGCAATC ATGGCTCACT 2450
|
